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Resource Name Proper Citation Abbreviations Resource Type Description Keywords Resource Relationships Related Condition Funding Defining Citation Availability Specification URL Alternate IDs Alternate URLs Old URLs Parent Organization Resource ID Synonyms Record Last Update Mentions Count
CDP
 
Resource Report
Resource Website
10+ mentions
CDP (RRID:SCR_004236) CDP funding resource, data or information resource, topical portal, portal National program to improve the diagnosis and assessment of cancer by moving scientific knowledge into clinical practice by coordinating and funding resources and research for the development of innovative in vitro diagnostics, novel diagnostic technologies and appropriate human specimens. The Cancer Diagnosis Program is divided into four branches: Biorepository and Biospecimen Research Branch (BBRB), Diagnostic Biomarkers and Technology Branch (DBTB), Diagnostics Evaluation Branch (DEB), and the Pathology Investigation and Resources Branch (PIRB). cancer research, cancer funding, cancer research funding is listed by: OMICtools
has parent organization: DCTD
Cancer NCI Available to cancer researchers OMICS_01536 SCR_004236 Cancer Diagnosis Program 2026-08-05 10:44:00 19
Taverna
 
Resource Report
Resource Website
10+ mentions
Taverna (RRID:SCR_004437) Taverna data processing software, software application, workflow software, software resource An open source and domain independent Workflow Management System ����?? a suite of tools used to design and execute scientific workflows and aid in silico experimentation. Taverna Workbench now has support for service sets, offline workflow editing, workflow validation, improved workflow run monitoring, and the pausing and canceling of workflow runs. The command line tool allows you to run workflows outside of the workbench and is available as a stand-alone download or bundled with the Taverna Workbench 2.2.0 download. The Taverna suite is written in Java and includes the Taverna Engine (used for enacting workflows) that powers both the Taverna Workbench (the desktop client application) and the Taverna Server (which allows remote execution of workflows). Taverna is also available as a Command Line Tool for a quick execution of workflows from a terminal. Taverna 2.2.0 includes * Copy/paste, shortcuts, undo/redo, drag and drop * Animated workflow diagram * Remembers added/removed services * Secure Web services support * Secure access to resources on the web * Up-to-date R support * Intermediate values during workflow runs * myExperiment integration * Excel and csv spreadsheet support * Command line tool is listed by: OMICtools
is listed by: SoftCite
is related to: myExperiment
is related to: U-Compare
is related to: Taverna Knowledge Blog
is related to: AIDA Toolkit
is related to: Knowledge Blog
has parent organization: University of Manchester; Manchester; United Kingdom
OMII-UK ;
EPSRC ;
BBSRC ;
Microsoft ;
ESRC ;
JISC
PMID:18337261
PMID:23640334
Open unspecified license nlx_43462, OMICS_01146 SCR_004437 2026-08-05 10:44:02 30
STAR
 
Resource Report
Resource Website
10000+ mentions
STAR (RRID:SCR_004463) data processing software, image analysis software, software application, alignment software, software resource Software performing alignment of high-throughput RNA-seq data. Aligns RNA-seq reads to reference genome using uncompressed suffix arrays. RNA-seq data, alignment, RNA-seq reads alignment, reference genome, using uncompressed suffix arrays, bio.tools is used by: STARsolo
is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
is listed by: SoftCite
NHGRI U54 HG004557 PMID:23104886
DOI:10.1093/bioinformatics/bts635
biotools:star, OMICS_01254, SCR_015899 https://github.com/alexdobin/STAR, https://bio.tools/star, https://sources.debian.org/src/rna-star/ SCR_004463 Spliced Transcripts Alignment to Reference, Spliced Transcripts Alignment to a Reference (STAR), rna-star, ultrafast universal RNA-seq aligner 2026-08-05 10:44:03 22809
QuickGO
 
Resource Report
Resource Website
500+ mentions
QuickGO (RRID:SCR_004608) QuickGO data or information resource, controlled vocabulary, data access protocol, database, software resource, ontology, web service A web-based browser for Gene Ontology terms and annotations, which is provided by the UniProtKB-GOA group at the EBI. It is able to offer a range of facilities including bulk downloads of GO annotation data which can be extensively filtered by a range of different parameters and GO slim set generation. The software for QuickGO is freely available under the Apache 2 license. QuickGO can supply GO term information and GO annotation data via REST web services. gene, ontology, annotation, browser, visualization, search engine, slimmer-type tool, ontology or annotation browser, ontology or annotation search engine, ontology or annotation visualization, database or data warehouse, windows, mac os x, linux, unix, gold standard, bio.tools is listed by: OMICtools
is listed by: Gene Ontology Tools
is listed by: bio.tools
is listed by: Debian
is related to: Gene Ontology
is related to: STRAP
has parent organization: European Bioinformatics Institute
BBSRC BB/E023541/1 PMID:19744993
PMID:20157483
Apache License, v2, Free for academic use biotools:quickgo, nlx_60318, OMICS_02276 https://bio.tools/quickgo SCR_004608 Quick GO 2026-08-05 10:44:04 523
ShotGun
 
Resource Report
Resource Website
10+ mentions
ShotGun (RRID:SCR_002529) data processing software, software application, simulation software, data analysis software, sequence analysis software, software resource Software for short read simulating in order to facilitate sequencing-based study designs. sequence based study design, short read stimulation, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
has parent organization: University of North Carolina at Chapel Hill; North Carolina; USA
PMID:23357921 Free, Available for download, Freely available biotools:abcd, OMICS_00255 https://bio.tools/abcd SCR_002529 ShotGun: a Flexible Short Read Simulator to Facilitate Sequencing-based Study Designs 2026-08-05 10:43:38 32
Gibbs Motif Sampler
 
Resource Report
Resource Website
1+ mentions
Gibbs Motif Sampler (RRID:SCR_002550) Gibbs Motif Sampler software resource, data analysis service, production service resource, service resource, analysis service resource Software to identify motifs, conserved regions, in DNA or protein sequences. dna, protein, motif, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
Free, Available for download, Freely available biotools:gibbs_motif_sampler, OMICS_00496 https://bio.tools/gibbs_motif_sampler SCR_002550 The Gibbs Motif Sampler 2026-08-05 10:43:39 2
NCBI database of Genotypes and Phenotypes (dbGap)
 
Resource Report
Resource Website
500+ mentions
NCBI database of Genotypes and Phenotypes (dbGap) (RRID:SCR_002709) dbGaP data or information resource, data repository, database, storage service resource, service resource Database developed to archive and distribute clinical data and results from studies that have investigated interaction of genotype and phenotype in humans. Database to archive and distribute results of studies including genome-wide association studies, medical sequencing, molecular diagnostic assays, and association between genotype and non-clinical traits. clinical, trial, genotype, interaction, homology, cell, morphology, interaction, phenotype, molecular diagnosis, genetic recombination, gold standard, bio.tools is used by: International Genomics of Alzheimers Project
is used by: NIDDK Inflammatory Bowel Disease Genetics Consortium
is used by: NIH Heal Project
is used by: Genomic Data Commons Data Portal (GDC Data Portal)
is recommended by: National Library of Medicine
is recommended by: NIDDK Information Network (dkNET)
is recommended by: NIDDK - National Institute of Diabetes and Digestive and Kidney Diseases
is listed by: OMICtools
is listed by: re3data.org
is listed by: NIDDK Information Network (dkNET)
is listed by: bio.tools
is listed by: Debian
is related to: NIDDK Central Repository
is related to: eMERGE Network: electronic Medical Records and Genomics
is related to: Framingham Heart Study
is related to: PhenoExplorer
is related to: Chronic Renal Insufficiency Cohort Study
is related to: DbGaP Cleaner
is related to: Psychiatric Genomics Consortium
is related to: ISCA Consortium
is related to: Allen Institute for Brain Science
has parent organization: NCBI
is parent organization of: Resource for Genetic Epidemiology Research on Adult Health and Aging
NLM PMID:24297256
PMID:17898773
Restricted nif-0000-23342, OMICS_00263, biotools:dbgap, r3d100010788 http://www.ncbi.nlm.nih.gov/sites/entrez?db=gap, https://bio.tools/dbgap, https://doi.org/10.17616/R3GS4K SCR_002709 database of Genotypes and Phenotypes (dbGaP), dbGaP, NCBI, Database of Genotypes and Phenotypes 2026-08-05 10:43:40 683
BioStar
 
Resource Report
Resource Website
50+ mentions
BioStar (RRID:SCR_002580) Biostar data or information resource, narrative resource, portal, forum, community building portal, discussion A question answer forum for scientists, focusing on methods in bioinformatics, computational genomics and biological data analysis. They welcome detailed and specific posts, written clearly and simply. bioinformatics, computational genomics, biological data analysis, data analysis, forum, question, answer is listed by: OMICtools
is related to: NeuroStars
NIH ;
Luma Education ;
NHGRI 5R25HG006243-02
PMID:22046109 Free, Freely available OMICS_01706, nlx_155982 SCR_002580 biostars.org 2026-08-05 10:43:38 84
discoSnp
 
Resource Report
Resource Website
1+ mentions
discoSnp (RRID:SCR_002612) data processing software, software application, sequence analysis software, data analysis software, software resource Software designed for discovering Single Nucleotide Polymorphism (SNP) from raw sets of reads obtained with Next Generation Sequencers (NGS). single nucleotide polymorphism, snp discovery, discover snp, bio.tools is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
SOFIPROTEOL under the FASO project PEAPOL ;
INRIA ANR-12-BS02-0008
PMID:25404127 Free, Freely available biotools:discosnp, OMICS_00267 https://bio.tools/discosnp, https://sources.debian.org/src/discosnp/ SCR_002612 DiscoSnp++, discovering Single Nucleotide Polymorphism, discovering Single Nucleotide Polymorphism (discoSNP) 2026-08-05 10:43:40 9
CTF
 
Resource Report
Resource Website
1+ mentions
CTF (RRID:SCR_002692) data processing software, software application, sequence analysis software, data analysis software, software resource Conditional random field (CRF) based transcription factor binding site (TFBS) finding system. The underlying CRF model can integrate features of different sources. conditional random field, transcription factor binding site, finding system, find transcription factor binding site is listed by: OMICtools
has parent organization: Shanghai Jiao Tong University; Shanghai; China
Free, Available for download, Freely available OMICS_00480 SCR_002692 2026-08-05 10:43:40 1
Rainbow
 
Resource Report
Resource Website
10+ mentions
Rainbow (RRID:SCR_002724) data processing software, software application, sequence analysis software, data analysis software, software resource Software developed to provide an ultra-fast and memory-efficient solution to clustering and assembling short reads produced by RAD-seq. software, tool, clustering, assembling, short, read, restriction, site, DNA, sequence, analysis, bio.tools is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
has parent organization: SourceForge
PMID:22942077
DOI:10.1093/bioinformatics/bts482
Free, Freely available, Available for download SCR_015992, OMICS_03722, biotools:rainbow https://bio.tools/rainbow, https://sources.debian.org/src/bio-rainbow/ SCR_002724 RAD-seq: Restriction-site Associated DNA sequencing, Bio-rainbow, RAD-seq 2026-08-05 10:43:41 41
PharmGKB
 
Resource Report
Resource Website
1000+ mentions
PharmGKB (RRID:SCR_002689) PharmGKB data or information resource, data repository, data access protocol, data set, database, software resource, storage service resource, service resource, web service Database and central repository for genetic, genomic, molecular and cellular phenotype data and clinical information about people who have participated in pharmacogenomics research studies. The data includes, but is not limited to, clinical and basic pharmacokinetic and pharmacogenomic research in the cardiovascular, pulmonary, cancer, pathways, metabolic and transporter domains. PharmGKB welcomes submissions of primary data from all research into genes and genetic variation and their effects on drug and disease phenotypes. PharmGKB collects, encodes, and disseminates knowledge about the impact of human genetic variations on drug response. They curate primary genotype and phenotype data, annotate gene variants and gene-drug-disease relationships via literature review, and summarize important PGx genes and drug pathways. PharmGKB is part of the NIH Pharmacogenomics Research Network (PGRN), a nationwide collaborative research consortium. Its aim is to aid researchers in understanding how genetic variation among individuals contributes to differences in reactions to drugs. A selected subset of data from PharmGKB is accessible via a SOAP interface. Downloaded data is available for individual research purposes only. Drugs with pharmacogenomic information in the context of FDA-approved drug labels are cataloged and drugs with mounting pharmacogenomic evidence are listed. pharmacogenomics, microarray, pathway, phenotype, snp array, genotype, clinical, genetic variation, drug, gene, genetic variation, disease, cardiovascular, pulmonary, cancer, metabolic, transporter, drug response, small molecule, research, drug response, FASEB list is used by: NIF Data Federation
is listed by: OMICtools
is related to: WikiPathways
is related to: ConsensusPathDB
is related to: Integrated Molecular Interaction Database
is related to: MalaCards
is related to: phenomeNET
has parent organization: Stanford University; Stanford; California
is parent organization of: PharmGKB Ontology
NIGMS R24 GM61374 PMID:11908751 Free, Freely available nif-0000-00414, OMICS_01586, r3d100012325 https://doi.org/10.17616/R31H1N SCR_002689 Pharmacogenomics Knowledge Base 2026-08-05 10:43:40 1152
pIRS
 
Resource Report
Resource Website
50+ mentions
pIRS (RRID:SCR_002519) software application, simulation software, software resource Software for de novo data simulation. It uses empirical distribution to reproduce Illumina pair-end reads with real distribution of substitution sequencing errors, quality values and GC%-depth bias. de novo data simulation, empirical distribution, illumina pair-end read, substitution sequencing error, gc depth bias is listed by: OMICtools PMID:22508794 Free, Available for download, Freely available OMICS_00254 SCR_002519 pIRS (profile based Illumina pair-end Reads Simulator), profile based Illumina pair-end Reads Simulator 2026-08-05 10:43:37 74
Gene Ontology
 
Resource Report
Resource Website
10000+ mentions
Gene Ontology (RRID:SCR_002811) GO data or information resource, portal, project portal, consortium, organization portal, knowledge environment resource Computable knowledge regarding functions of genes and gene products. GO resources include biomedical ontologies that cover molecular domains of all life forms as well as extensive compilations of gene product annotations to these ontologies that provide largely species-neutral, comprehensive statements about what gene products do. Used to standardize representation of gene and gene product attributes across species and databases. gene, product, annotation, molecular, function, cellular, biological, role, database, query, obo, gold standard, bio.tools, FASEB list is used by: NIF Data Federation
is used by: GreenPhylDB
is used by: LIPID MAPS Proteome Database
is used by: Aging Portal
is used by: ChannelPedia
is used by: Open PHACTS
is used by: CoPub
is used by: PhenoGO
is used by: Database for Annotation Visualization and Integrated Discovery
is used by: MitoMiner
is used by: dcGO
is used by: Pathway Analysis Tool for Integration and Knowledge Acquisition
is used by: barleyGO
is used by: SynGO
is used by: Functional Annotation
is used by: SwissLipids
is listed by: BioPortal
is listed by: OBO
is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
is affiliated with: Mouse Genome Informatics: The Gene Ontology Project
is related to: GenNav
is related to: SynaptomeDB
is related to: High-Throughput GoMiner
is related to: Onto-Design
is related to: OnEx - Ontology Evolution Explorer
is related to: Avadis
is related to: GONUTS
is related to: PiNGO
is related to: Automated Microarray Pipeline
is related to: categoryCompare
is related to: globaltest
is related to: Semantic Measures Library
is related to: WegoLoc
is related to: AnimalTFDB
is related to: MEME Suite - Motif-based sequence analysis tools
is related to: Arabidopsis Hormone Database
is related to: DAVID
is related to: Arabidopsis thaliana Protein Interactome Database
is related to: TM4 Microarray Software Suite - TIGR MultiExperiment Viewer
is related to: pSTIING
is related to: GoMiner
is related to: FunSimMat
is related to: GeneSpeed- A Database of Unigene Domain Organization
is related to: Centre for Modeling Human Disease Gene Trap Resource
is related to: Patterns of Gene Expression in Drosophila Embryogenesis
is related to: Babelomics
is related to: BioPerl
is related to: GeneCruiser
is related to: GOLEM An interactive, graphical gene-ontology visualization, navigation, and analysis tool
is related to: GOToolBox Functional Investigation of Gene Datasets
is related to: Cotton EST Database
is related to: MouseNET
is related to: PLANTTFDB
is related to: T-profiler
is related to: Physico-Chemical Process
is related to: Integrated Molecular Interaction Database
is related to: SEGS
is related to: GOCat
is related to: Quantitative Enrichment of Sequence Tags
is related to: Neural-Immune Gene Ontology
is related to: INMEX
is related to: StRAnGER
is related to: QuickGO
is related to: Repository of molecular brain neoplasia data
is related to: Cardiovascular Gene Ontology Annotation Initiative
is related to: PANTHER
is related to: Short Time-series Expression Miner (STEM)
is related to: DATFAP
is related to: GORetriever
is related to: Gene Ontology Browsing Utility (GOBU)
is related to: GeneTools
is related to: GOSlimViewer
is related to: go-moose
is related to: Network Ontology Analysis
is related to: Onto-Compare
is related to: Onto-Express
is related to: OntoVisT
is related to: STRAP
is related to: CGAP GO Browser
is related to: COBrA
is related to: Gene Class Expression
is related to: GeneInfoViz
is related to: GOfetcher
is related to: GoFish
is related to: GOProfiler
is related to: GOanna
is related to: Manatee
is related to: Pandora - Protein ANnotation Diagram ORiented Analysis
is related to: TAIR Keyword Browser
is related to: Wandora
is related to: GOTaxExplorer
is related to: Onto-Miner
is related to: Onto-Translate
is related to: ToppGene Suite
is related to: DBD - Slim Gene Ontology
is related to: ONTO-PERL
is related to: Blip: Biomedical Logic Programming
is related to: OWL API
is related to: CLENCH
is related to: BiNGO: A Biological Networks Gene Ontology tool
is related to: CateGOrizer
is related to: FuSSiMeG: Functional Semantic Similarity Measure between Gene-Products
is related to: ProteInOn
is related to: GeneMerge
is related to: GraphWeb
is related to: ClueGO
is related to: CLASSIFI - Cluster Assignment for Biological Inference
is related to: GOHyperGAll
is related to: FuncAssociate: The Gene Set Functionator
is related to: GOdist
is related to: FuncExpression
is related to: FunCluster
is related to: FIVA - Functional Information Viewer and Analyzer
is related to: GARBAN
is related to: GOEx - Gene Ontology Explorer
is related to: SGD Gene Ontology Slim Mapper
is related to: GOArray
is related to: SNPsandGO
is related to: GoSurfer
is related to: GOtcha
is related to: MAPPFinder
is related to: GoAnnotator
is related to: MetaGeneProfiler
is related to: OntoGate
is related to: ProfCom - Profiling of complex functionality
is related to: SerbGO
is related to: SOURCE
is related to: Ontologizer
is related to: THEA - Tools for High-throughput Experiments Analysis
is related to: Generic GO Term Mapper
is related to: GREAT: Genomic Regions Enrichment of Annotations Tool
is related to: GoBean - a Java application for Gene Ontology enrichment analysis
is related to: TXTGate
is related to: GO-Module
is related to: IT-GOM: Integrated Tool for IC-based GO Semantic Similarity Measures
is related to: G-SESAME - Gene Semantic Similarity Analysis and Measurement Tools
is related to: MalaCards
is related to: FSST - Functional Similarity Search Tool
is related to: Expression Profiler
is related to: GOChase
is related to: GoPubMed
is related to: Whatizit
is related to: REViGO
is related to: WEGO - Web Gene Ontology Annotation Plot
is related to: Blast2GO
is related to: InterProScan
is related to: PubSearch
is related to: TrED
is related to: CharProtDB: Characterized Protein Database
is related to: VirHostNet: Virus-Host Network
is related to: Pathbase
is related to: GO Online SQL Environment (GOOSE)
is related to: Neurobehavior Ontology
is related to: InterSpecies Analysing Application using Containers
is related to: KOBAS
is related to: ConceptWiki
is related to: GeneTerm Linker
is related to: Bioconductor
is related to: ErmineJ
is related to: Gene Ontology For Functional Analysis (GOFFA)
is related to: MGI GO Browser
is related to: Comparative Toxicogenomics Database (CTD)
is related to: GOEAST - Gene Ontology Enrichment Analysis Software Toolkit
is related to: Ontology Lookup Service
is related to: LexGrid
is related to: WebGestalt: WEB-based GEne SeT AnaLysis Toolkit
is related to: g:Profiler
is related to: OwlSim
is related to: GOrilla: Gene Ontology Enrichment Analysis and Visualization Tool
is related to: YeTFaSCo
is related to: FastSemSim
is related to: RamiGO
is related to: AutismKB
is related to: GeneCodis
is related to: FunSpec
is related to: FunNet - Transcriptional Networks Analysis
is related to: PhenoM - Phenomics of yeast Mutants
is related to: agriGO
is related to: GOblet
is related to: DynGO
is related to: SeqExpress
is related to: ProbeExplorer
is related to: ECgene: Gene Modeling with Alternative Splicing
is related to: Organelle DB
is related to: Gemma
is related to: Candidate Genes to Inherited Diseases
is related to: Proteome Analyst PA-GOSUB
is related to: Network Analysis, Visualization and Graphing TORonto
is related to: GOstat
is related to: Onto-Express To Go (OE2GO)
is related to: Tk-GO
is related to: EGAN: Exploratory Gene Association Networks
is related to: Spotfire
is related to: GOMO - Gene Ontology for Motifs
is related to: GFINDer: Genome Function INtegrated Discoverer
is related to: Generic GO Term Finder
is related to: Agile Protein Interactomes DataServer
is related to: AgingDB
is related to: UBERON
is related to: Algal Functional Annotation Tool
is related to: gsGator
is related to: Flash Gviewer
is related to: Cerebellar Development Transcriptome Database
is related to: PlantNATsDB - Plant Natural Antisense Transcripts DataBase
is related to: EASE: the Expression Analysis Systematic Explorer
is related to: PiGenome
is related to: L2L Microarray Analysis Tool
is related to: MeGO
is related to: CELDA Ontology
is related to: Diabetes Disease Portal
is related to: MatrixDB
is related to: Kidney and Urinary Pathway Knowledge Base
is related to: MouseCyc
is related to: Candida Genome Database
is related to: Honey Bee Brain EST Project
is related to: ECO
is related to: FlyMine
is related to: Gramene
is related to: 3D-Interologs
is related to: Biomine
is related to: UniProtKB
is related to: NCBI BioSystems Database
is related to: EBIMed
is related to: Coremine Medical
is related to: EMAGE Gene Expression Database
is related to: GeneMANIA
is related to: Yeast Search for Transcriptional Regulators And Consensus Tracking
is related to: GeneTrail
is related to: Magic
is related to: Mouse Genome Informatics (MGI)
is related to: FlyBase
is related to: InterPro
is related to: InnateDB
is related to: canSAR
is related to: HPRD - Human Protein Reference Database
is related to: CRCView
is related to: Integrated Manually Extracted Annotation
is related to: LegumeIP
is related to: Renal Disease Portal
is related to: PhenoGO
is related to: DOAF
is related to: OBO
is related to: biomaRt
is related to: OncoboxPD
is parent organization of: AmiGO
is parent organization of: GOlr
is parent organization of: RefGenome
is parent organization of: OBO-Edit
is parent organization of: OWLTools
is parent organization of: Gene Ontology Tools
is parent organization of: Gene Ontology Extension
is parent organization of: SO
is parent organization of: go-db-perl
is parent organization of: go-perl
works with: topGO
works with: DIANA-mirPath
works with: GOnet
is organization facet of: Alliance of Genome Resources
European Union QLRI-CT-2001-0098;
European Union QLRI-CT-2001-00015;
NHGRI P41 HG002273
PMID:23161678
PMID:10802651
Free, Freely available, Available for download biotools:go, OMICS_02278, nif-0000-02915 http://bioportal.bioontology.org/ontologies/GO, https://bio.tools/go SCR_002811 the Gene Ontology, GO, Gene Ontology Resource, Gene Ontology 2026-08-05 10:43:41 10623
RNA Abundance Database
 
Resource Report
Resource Website
1+ mentions
RNA Abundance Database (RRID:SCR_002771) RAD data or information resource, data repository, database, storage service resource, resource, service resource THIS RESOURCE IS NO LONGER IN SERVICE, Documented on March 24, 2014. A resource for gene expression studies, storing highly curated MIAME-compliant studies (i.e. experiments) employing a variety of technologies such as filter arrays, 2-channel microarrays, Affymetrix chips, SAGE, MPSS and RT-PCR. Data were available for querying and downloading based on the MGED ontology, publications or genes. Both public and private studies (the latter viewable only by users having appropriate logins and permissions) were available from this website. Specific details on protocols, biomaterials, study designs, etc., are collected through a user-friendly suite of web annotation forms. Software has been developed to generate MAGE-ML documents to enable easy export of studies stored in RAD to any other database accepting data in this format. RAD is part of a more general Genomics Unified Schema (http://gusdb.org), which includes a richly annotated gene index (http://allgenes.org), thus providing a platform that integrates genomic and transcriptomic data from multiple organisms. NOTE: Due to changes in technology and funding, the RAD website is no longer available. RAD as a schema is still very much active and incorporated in the GUS (Genomics Unified Schema) database system used by CBIL (EuPathDB, Beta Cell Genomics) and others. The schema for RAD can be viewed along with the other GUS namespaces through our Schema Browser. gene expression, gene, affymetrix, biomaterial, genomics, microarray, mpss, ontology, rna, rt-pcr, sage, functional genomics, transcript abundance is listed by: OMICtools
is related to: MIAME
is related to: MGED Ontology
is related to: MicroArray and Gene Expression Markup Language
has parent organization: University of Pennsylvania; Philadelphia; USA
NIH ;
NHGRI RO1-HG-01539;
NIDDK U01DK56947;
NHGRI K25-HG-02296;
NHGRI K25-HG-00052
THIS RESOURCE IS NO LONGER IN SERVICE nif-0000-00133, OMICS_00869, r3d100000017 https://doi.org/10.17616/R3QP4Q SCR_002771 RNA Abundance Database 2026-08-05 10:43:41 4
IMEx - The International Molecular Exchange Consortium
 
Resource Report
Resource Website
100+ mentions
IMEx - The International Molecular Exchange Consortium (RRID:SCR_002805) IMEx data or information resource, data repository, portal, consortium, community building portal, database, organization portal, storage service resource, service resource Interaction database from international collaboration between major public interaction data providers who share curation effort and develop set of curation rules when capturing data from both directly deposited interaction data or from publications in peer reviewed journals. Performs complete curation of all protein-protein interactions experimentally demonstrated within publication and makes them available in single search interface on common website. Provides data in standards compliant download formats. IMEx partners produce their own separate resources, which range from all encompassing molecular interaction databases, such as are maintained by IntAct, MINT and DIP, organism-centric resources such as BioGrid or MPIDB or biological domain centric, such as MatrixDB. They have committed to making records available, via PSICQUIC webservice, which have been curated to IMEx rules and are available to users as single, non-redundant set of curated publications which can be searched at the IMEx website. Data is made available in standards-compliant tab-deliminated and XML formats, enabling to visualize data using wide range of tools. Consortium is open to participation of additional partners and encourages deposition of data, prior to publication, and will supply unique accession numbers which may be referenced within final article. Submitters may send their data directly to any of member databases using variety of formats, but should conform to guidelines as to minimum information required to describe data. protein-protein interaction, nonredundant, protein interaction, interaction, proteomics, metadata standard, short course, molecular interaction, bio.tools, FASEB list is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
is affiliated with: MINT
is related to: MatrixDB
is related to: MPIDB
is related to: Database of Interacting Proteins (DIP)
is related to: Database of Interacting Proteins (DIP)
is related to: InnateDB
is related to: IntAct
is related to: Interaction Reference Index
is related to: MPIDB
is related to: UniProt
is related to: InnateDB
is related to: MatrixDB
is related to: Biological General Repository for Interaction Datasets (BioGRID)
is related to: I2D
is related to: Molecular Connections NetPro
is related to: SIB Swiss Institute of Bioinformatics
is related to: IntAct
is related to: PSI-MI
is related to: PSICQUIC Registry
is related to: mentha
is related to: Bioconductor
has parent organization: European Bioinformatics Institute
works with: CellPhoneDB
works with: Cytoscape
works with: IntAct
works with: MINT
works with: MPact: Representation of Interaction Data at MIPS
works with: Molecular Connections NetPro
works with: Biological General Repository for Interaction Datasets (BioGRID)
works with: InnateDB
works with: BIND
European Union PMID:22453911
PMID:17893861
Free, Freely available, Available for download nif-0000-00447, OMICS_01545, r3d100010669, biotools:imex http://imex.sourceforge.net/, https://bio.tools/imex, https://doi.org/10.17616/R3090W SCR_002805 The International Molecular Exchange Consortium, International Molecular Exchange Consortium 2026-08-05 10:43:41 144
ANDES
 
Resource Report
Resource Website
10+ mentions
ANDES (RRID:SCR_002791) data processing software, software application, data analysis software, software toolkit, software resource Software library and a suite of applications, written in Perl and R, for deep sequencing statistical analyses. deep sequencing, biomarker detection, statistical analysis, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
has parent organization: SourceForge
PMID:20633290 Free, Freely available, Available for download biotools:andes, OMICS_01119 https://bio.tools/andes SCR_002791 Statistical tools for the Analyses of Deep Sequencing (ANDES), Statistical tools for the Analyses of Deep Sequencing, Statistical tools for the ANalyses of Deep Sequencing 2026-08-05 10:43:41 25
R-pbh5
 
Resource Report
Resource Website
R-pbh5 (RRID:SCR_003026) software toolkit, software library, software resource Software library for accessing data in HDF5 files produced by Pacific Biosciences sequencing machines. The R package supports accessing data from: cmp.h5, bas.h5, pls.h5, and trc.h5. software package, r is listed by: OMICtools Free, Available for download, Freely available OMICS_05139 https://github.com/extemporaneousb/R-pbh5 SCR_003026 2026-08-05 10:43:45 0
ArrayExpress
 
Resource Report
Resource Website
5000+ mentions
ArrayExpress (RRID:SCR_002964) ArrayExpress data or information resource, data repository, catalog, database, storage service resource, service resource International functional genomics data collection generated from microarray or next-generation sequencing (NGS) platforms. Repository of functional genomics data supporting publications. Provides genes expression data for reuse to the research community where they can be queried and downloaded. Integrated with the Gene Expression Atlas and the sequence databases at the European Bioinformatics Institute. Contains a subset of curated and re-annotated Archive data which can be queried for individual gene expression under different biological conditions across experiments. Data collected to MIAME and MINSEQE standards. Data are submitted by users or are imported directly from the NCBI Gene Expression Omnibus. gold, standard, functional, genomics, data, collection, microarray, next, generation, sequencing, NGS, repository uses: MIAME
uses: MINSEQE
uses: Gene Expression Omnibus
is used by: NIF Data Federation
is used by: BioSample Database at EBI
is used by: Integrated Datasets
is recommended by: NIDDK Information Network (dkNET)
is recommended by: NIDDK - National Institute of Diabetes and Digestive and Kidney Diseases
is listed by: DataCite
is listed by: OMICtools
is listed by: re3data.org
is related to: DDBJ Omics Archive
is related to: MIAME
is related to: Gene Expression Atlas
is related to: Experimental Factor Ontology
is related to: Bgee: dataBase for Gene Expression Evolution
is related to: ISA Infrastructure for Managing Experimental Metadata
is related to: FlyMine
is related to: MAGE-TAB
is related to: Experimental Factor Ontology
is related to: Magic
is related to: ArrayExpress (R)
is related to: CancerMIRNome
has parent organization: European Bioinformatics Institute
European Union ;
SLING 226073;
European Commission ;
Gen2Phen 200754;
NHGRI P41 HG003619
PMID:23193272
PMID:21071405
Available Public or Private, Free, Available for download, The community can contribute to this resource, Acknowledgement requested, to access private data registration required OMICS_01023, nif-0000-30123, r3d100010222 http://www.ebi.ac.uk/microarray-as/ae, https://doi.org/10.17616/R3302G SCR_002964 , ArrayExpress, ArrayExpress - functional genomics data, ArrayExpress Archive 2026-08-05 10:43:44 7529
GenBank
 
Resource Report
Resource Website
10000+ mentions
GenBank (RRID:SCR_002760) GB data or information resource, data repository, database, storage service resource, service resource NIH genetic sequence database that provides annotated collection of all publicly available DNA sequences for almost 280 000 formally described species (Jan 2014) .These sequences are obtained primarily through submissions from individual laboratories and batch submissions from large-scale sequencing projects, including whole-genome shotgun (WGS) and environmental sampling projects. Most submissions are made using web-based BankIt or standalone Sequin programs, and GenBank staff assigns accession numbers upon data receipt. It is part of International Nucleotide Sequence Database Collaboration and daily data exchange with European Nucleotide Archive (ENA) and DNA Data Bank of Japan (DDBJ) ensures worldwide coverage. GenBank is accessible through NCBI Entrez retrieval system, which integrates data from major DNA and protein sequence databases along with taxonomy, genome, mapping, protein structure and domain information, and biomedical journal literature via PubMed. BLAST provides sequence similarity searches of GenBank and other sequence databases. Complete bimonthly releases and daily updates of GenBank database are available by FTP. genetic sequence, dna sequence, human genetics, human genome, nucleotide sequence, nucleotide, dna, dna data bank, gene mapping, genetics, gold standard is used by: Structural Genomics Consortium
is used by: xFITOM
is used by: Transcriptional Regulatory Element Database
is recommended by: National Library of Medicine
is recommended by: NIDDK Information Network (dkNET)
is recommended by: NIDDK - National Institute of Diabetes and Digestive and Kidney Diseases
is listed by: OMICtools
is listed by: re3data.org
is listed by: CINERGI
is related to: High Throughput Genomic Sequences Division
is related to: DNA DataBank of Japan (DDBJ)
is related to: HS3D - Homo Sapiens Splice Sites Dataset
is related to: Influenza Virus Resource
is related to: TPA
is related to: Anopheles gambiae (African malaria mosquito) genome view
is related to: Nucleotide database
is related to: NCBI BioSample
is related to: NCBI Nucleotide
is related to: SpliceDB
is related to: MaizeGDB
is related to: NCBI Assembly Archive Viewer
is related to: DNA DataBank of Japan (DDBJ)
is related to: European Molecular Biology Laboratory
is related to: INSDC
is related to: NCBI Protein Database
is related to: TrED
is related to: Xenopus Gene Collection
is related to: Mammalian Gene Collection
is related to: Zebrafish Gene Collection
is related to: INSDC
is related to: NCBI Virus
is related to: Codon and Codon-Pair Usage Tables
has parent organization: NCBI
is parent organization of: NCBI Genome Survey Sequences Database
is parent organization of: NCBI Genome Survey Sequences Database
works with: OGDraw
works with: A plasmid Editor
works with: Webcutter
works with: merge-gbk-records
works with: PremierBiosoft Proteo IQ Software
works with: SARS-CoV-2-Sequences
works with: rentrez
works with: MiMeDB
NLM PMID:24217914
PMID:23193287
PMID:21071399
Free, Freely available nif-0000-02873, r3d100010528, OMICS_01650 https://doi.org/10.17616/R3D31X SCR_002760 , Gen Bank, GenBank 2026-08-05 10:43:41 61478

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